
An
amino acid, in its (1) normal (unionized) and (2) zwitterionic forms.
A 'zwitterion' (from
German "''Zwitter''" — "hybrid," "
hermaphrodite") is a
chemical compound that is electrically neutral but carries formal positive and negative charges on different
atoms.
[1] Zwitterions are
polar and usually have a high solubility in water and a poor solubility in most
organic solvents.
'Ampholytes' are molecules that contain both
acidic and
basic groups (and are therefore
amphoteric) and will exist as zwitterions at a certain
pH. This pH is known as the molecule's
isoelectric point. Ampholytic molecules make good
buffer solutions — they resist change to the pH of a solution by selective ionization. In the presence of acids, they will accept the hydrogen ions, removing them from the solution. In the presence of
bases, they will donate hydrogen ions to the solution, again balancing the pH.
Typical examples of zwitterions are:
★ Used as
buffering agents most of which are included in
Good's buffers:
★
★ The amino-
sulfonic acid based
MES,
MOPS,
HEPES,
PIPES or
CAPS
★
★ The amino-
carboxylic acid (
amino acid) based
glycine, its derivatives
bicine and
tricine, and
alanine
★ Used as
detergents:
★
★
CHAPSO
★ Natural products like the
alkaloids
psilocybin and
lysergic acid.
★
Betaines
Less common examples of zwitterions are:
★
Quinonoid zwitterions.
★ Drugs such as
Fexofenadine (Allegra®).
References
1. Compendium of Chemical Terminology, zwitterion